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The role of T cells in osteoporosis, an update.T细胞在骨质疏松症中的作用:最新进展
Int J Clin Exp Pathol. 2009 May 20;2(6):544-52.
2
T cells: unexpected players in the bone loss induced by estrogen deficiency and in basal bone homeostasis.T细胞:雌激素缺乏诱导的骨质流失及基础骨稳态中的意外参与者。
Ann N Y Acad Sci. 2007 Nov;1116:360-75. doi: 10.1196/annals.1402.068.
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The role of the immune system in the physiopathology of osteoporosis.免疫系统在骨质疏松症病理生理学中的作用。
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The role of T lymphocytes in bone metabolism.T淋巴细胞在骨代谢中的作用。
Immunol Rev. 2005 Dec;208:154-68. doi: 10.1111/j.0105-2896.2005.00324.x.
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Estrogen deficiency, T cells and bone loss.雌激素缺乏、T细胞与骨质流失。
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Turbo methanol extract inhibits bone resorption through regulation of T cell function.涡轮甲醇提取物通过调节 T 细胞功能抑制骨吸收。
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Bone. 2008 Jul;43(1):92-100. doi: 10.1016/j.bone.2008.02.017. Epub 2008 Mar 7.
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Estrogen deficiency and bone loss: an inflammatory tale.雌激素缺乏与骨质流失:一个炎症故事。
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Increased Peripheral Blood Pro-Inflammatory/Cytotoxic Lymphocytes in Children with Bronchiectasis.支气管扩张症患儿外周血促炎/细胞毒性淋巴细胞增加。
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本文引用的文献

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In vivo activated monocytes from the site of inflammation in humans specifically promote Th17 responses.在人体内,来自炎症部位的体内活化单核细胞可特异性促进Th17反应。
Proc Natl Acad Sci U S A. 2009 Apr 14;106(15):6232-7. doi: 10.1073/pnas.0808144106. Epub 2009 Mar 26.
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Bidirectional signaling through ephrinA2-EphA2 enhances osteoclastogenesis and suppresses osteoblastogenesis.通过 EphrinA2-EphA2 的双向信号传导增强破骨细胞生成并抑制成骨细胞生成。
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Selective inhibition of RANK blocks osteoclast maturation and function and prevents bone loss in mice.对RANK的选择性抑制可阻断破骨细胞的成熟和功能,并防止小鼠骨质流失。
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Synergism between tumor necrosis factor alpha and interleukin-17 to induce IL-23 p19 expression in fibroblast-like synoviocytes.肿瘤坏死因子α与白细胞介素-17之间的协同作用可诱导成纤维样滑膜细胞中白细胞介素-23 p19的表达。
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Role of RANKL in bone diseases.核因子κB受体活化因子配体在骨疾病中的作用。
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The Src family kinase, Lyn, suppresses osteoclastogenesis in vitro and in vivo.Src家族激酶Lyn在体外和体内均抑制破骨细胞生成。
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RANK/RANKL: regulators of immune responses and bone physiology.RANK/RANKL:免疫反应和骨生理学的调节因子。
Ann N Y Acad Sci. 2008 Nov;1143:123-50. doi: 10.1196/annals.1443.016.
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Blockade of tumor necrosis factor in collagen-induced arthritis reveals a novel immunoregulatory pathway for Th1 and Th17 cells.在胶原诱导的关节炎中阻断肿瘤坏死因子揭示了Th1和Th17细胞的一种新的免疫调节途径。
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NFATc1 in mice represses osteoprotegerin during osteoclastogenesis and dissociates systemic osteopenia from inflammation in cherubism.小鼠中的NFATc1在破骨细胞生成过程中抑制骨保护素,并在 cherubism 中将全身性骨质减少与炎症分离。
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Bone marrow-based homeostatic proliferation of mature T cells in nonhuman primates: implications for AIDS pathogenesis.非人灵长类动物中成熟T细胞基于骨髓的稳态增殖:对艾滋病发病机制的影响。
Blood. 2009 Jan 15;113(3):612-21. doi: 10.1182/blood-2008-06-159442. Epub 2008 Oct 1.

T细胞在骨质疏松症中的作用:最新进展

The role of T cells in osteoporosis, an update.

作者信息

Zhao Wen, Liu Yuying, Cahill Catherine M, Yang Wenlu, Rogers Jack T, Huang Xudong

机构信息

Department of Orthopedics, Beijing Aerospace General Hospital Beijing, China.

出版信息

Int J Clin Exp Pathol. 2009 May 20;2(6):544-52.

PMID:19636401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2713452/
Abstract

Emerging evidence highlights the importance of the interplay between the bone and immune systems. That evidence bolsters a longstanding recognition that estrogen deficiency, infection, inflammation, and autoimmune disorders are associated with systemic and local bone loss. Yet, only recently has an understanding emerged that T lymphocytes and their products act as key regulators of osteoclast formation, life span, and activity. This review presents this understanding of the process of T lymphocytes and their products mediating osteoporosis and explores some of the most recent findings and hypotheses to explain their action in bone. A more complete appreciation of the interactions between immune and bone cells should lead to targeted therapeutic strategies for diseases that affect either or both systems.

摘要

新出现的证据凸显了骨骼与免疫系统之间相互作用的重要性。这一证据支持了长期以来的一种认识,即雌激素缺乏、感染、炎症和自身免疫性疾病与全身性和局部性骨质流失有关。然而,直到最近才认识到T淋巴细胞及其产物是破骨细胞形成、寿命和活性的关键调节因子。本综述阐述了对T淋巴细胞及其产物介导骨质疏松症过程的这一认识,并探讨了一些最新的发现和假说来解释它们在骨骼中的作用。对免疫细胞与骨细胞之间相互作用的更全面理解应该会为影响其中一个或两个系统的疾病带来有针对性的治疗策略。